Product Details

SNP ID: rs144643375
Assay Type: Functionally tested
NCBI dbSNP Submissions: 10
Location: Chr.1:152303006 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GACCTTTTTGCCTTTCAGTGCCCTC[A/G]GATTGATAATGATAAGAACTAGAAC
Phenotype: MIM: 135940
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: FLG PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002016.1	11916	Silent Mutation	TCC,TCT	S3960S	NP_002007.1